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Get the free Certificate of Confidentiality (CC) - SAMHSA

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Appendix A: Letter of participant consent to participate in CCB study CONSENT TO PARTICIPATE IN A STUDY Evaluation of Technology Creation and Use Workshops You have been asked to participate in a
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01
Determine if your research project meets the criteria for a Certificate of Confidentiality (CC). This includes having identifiable sensitive information that, if disclosed, could harm the research participants.
02
Fill out the application form provided by the funding agency or institution that issues CCs. Make sure to provide accurate and detailed information about your research project, the type of data collected, and how it will be protected.
03
Submit the completed application form along with any necessary supporting documents to the appropriate review board or office for approval.
04
Once approved, follow the guidelines and restrictions outlined in the CC regarding the use, disclosure, and protection of the sensitive data collected during your research.

Who needs certificate of confidentiality cc?

01
Researchers conducting studies that involve collecting sensitive and identifiable information about research participants are the ones who typically need a Certificate of Confidentiality (CC). This includes researchers in fields such as healthcare, psychology, social sciences, and biomedical research.
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A certificate of confidentiality (CoC) is a legal document issued by the National Institutes of Health (NIH) to protect identifiable, sensitive research information from being disclosed.
Researchers conducting studies that collect sensitive information are required to file a certificate of confidentiality.
Researchers can fill out the certificate of confidentiality form online through the NIH website.
The purpose of a certificate of confidentiality is to provide additional protection to researchers and their research subjects by safeguarding sensitive information.
The certificate of confidentiality must include details about the research study, the type of sensitive information being collected, and the procedures in place to protect the confidentiality of research participants.
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